Prekallikrein deficiency

MONDO:0044744

A condition characterized by the congenital or acquired deficiency of prekallikrein. This deficiency is usually not associated with bleeding. The congenital deficiency is very rare. Acquired deficiency may occur in diffuse intravascular coagulation, infections, and sickle cell disease.

Also known as: prekallikrein deficiency

3 clinical trials for this condition and its sub-types, 0 tagged with Prekallikrein deficiency itself.

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↑ Blood coagulation disease (541)

Sub-types of Prekallikrein deficiency

Inherited prekallikrein deficiency 0 trials

Including sub-types (3) Tagged with Prekallikrein deficiency (0)

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